ENST00000527168.6:n.853C>G
|
|
|
ENST00000529110.2:c.838C>G
|
ENSP00000435349.2:p.Leu280Val
|
|
ENST00000529957.6:n.812C>G
|
|
|
ENST00000683366.1:c.*486C>G
|
ENSP00000507283.1:n.*486C>G
|
|
ENST00000683887.1:c.802C>G
|
ENSP00000506886.1:p.Leu268Val
|
|
ENST00000684100.1:n.748C>G
|
|
|
ENST00000684126.1:n.888C>G
|
|
|
ENST00000684688.1:n.1379C>G
|
|
|
ENST00000204679.9:c.754C>G
MANE Select
|
ENSP00000204679.4:p.Leu252Val
|
|
ENST00000204679.8:c.754C>G
|
ENSP00000204679.4:p.Leu252Val
|
|
ENST00000527076.1:n.1977C>G
|
|
|
ENST00000527168.5:n.921C>G
|
|
|
ENST00000529957.5:n.853C>G
|
|
|
NM_032520.4:c.754C>G
|
NP_115909.1:p.Leu252Val
|
|
XM_017023782.1:c.802C>G
|
XP_016879271.1:p.Leu268Val
|
|
XM_017023783.1:c.394C>G
|
XP_016879272.1:p.Leu132Val
|
|
NM_032520.5:c.754C>G
MANE Select
|
NP_115909.1:p.Leu252Val
|
|